Identification of α‐Thalassemia Mutations in Iranian Individuals with Abnormal Hematological Indices and Normal Hb A₂

Ladan H. Gohari Iran University of Medical Sciences, Tehran, Iran

Miranda Petrou Senior Molecular Geneticist, Head, Molecular Genetics and Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus

Xenia Felekis Senior Molecular Geneticist, Head, Molecular Genetics and Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus

George Christopoulos Senior Molecular Geneticist, Head, Molecular Genetics and Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus

Marina Kleanthous Senior Molecular Geneticist, Head, Molecular Genetics and Thalassaemia Department, The Cyprus Institute of Neurology and Genetics, P.O. Box 23462, Nicosia, 1683, Cyprus

, Ph.D.

References

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Kyriacou K., Kyrri A., Kalogirou E., Vasiliades P., Angastiniotis M., Ioannou P. A., Kleanthous M. Hb Bart's levels in cord blood and α‐thalassemia mutations in Cyprus. Hemoglobin 2000; 24(3)171–180
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Identification of α‐Thalassemia Mutations in Iranian Individuals with Abnormal Hematological Indices and Normal Hb A₂

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Identification of α‐Thalassemia Mutations in Iranian Individuals with Abnormal Hematological Indices and Normal Hb A2

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Identification of α‐Thalassemia Mutations in Iranian Individuals with Abnormal Hematological Indices and Normal Hb A₂